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Franciscan Alliance, Inc.
Overview
The coordinator implements and completes clinical research protocols, including obtaining informed consent and performing protocol-specified procedures. They are responsible for recruiting subjects, maintaining documentation, and reporting adverse events to sponsors.
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Compensation
Salary not listed
Posted
1 month ago
Serv Recruitment Agency
The role involves supporting the day-to-day coordination of Phase I-III gynecologic oncology clinical trials, including managing regulatory files, tracking timelines, and coordinating patient visits and procedures. Responsibilities also include accurate data entry into EDC systems, maintaining audit-ready documentation, and assisting with regulatory compliance and monitoring visits.
2 months ago
Cedars-Sinai
The Clinical Research Coordinator II is responsible for independent study coordination, including assessing patient eligibility and managing documentation. They also compile and report study data and ensure compliance with regulatory standards.
4 months ago
